ICD-10 Code D80.0 | Hereditary hypogammaglobulinemia Symptoms, Diagnosis, Billing

Hereditary hypogammaglobulinemia is a genetic disorder characterized by low levels of immunoglobulins, leading to increased susceptibility to infections. This condition is crucial for accurate diagnosis and management, as it informs treatment strategies and preventive measures. The ICD-10 Code D80.0 facilitates precise documentation, billing, and public health reporting, ensuring that patients receive appropriate care and resources.

What is ICD-10 Code D80.0 for Hereditary hypogammaglobulinemia?

ICD-10 Code D80.0 represents hereditary hypogammaglobulinemia, a primary immunodeficiency disorder resulting from genetic defects affecting B-cell function. This code should be used in clinical documentation and billing when diagnosing patients with this condition, particularly when they present with recurrent infections or other related complications.

ICD-10 Code D80.0 – Clinical Definition and Explanation of Hereditary hypogammaglobulinemia

Hereditary hypogammaglobulinemia is caused by genetic mutations that impair the production of immunoglobulins, leading to a deficiency in antibody-mediated immunity. This condition can result in recurrent bacterial infections and requires prompt medical attention to prevent severe complications.

Key Clinical Features:

• Recurrent bacterial infections, particularly respiratory and gastrointestinal infections.
• Low serum immunoglobulin levels, especially IgG, IgA, and IgM.
• Family history of immunodeficiency disorders.
• Delayed or absent antibody response to vaccinations.

ICD-10 Code D80.0 for Hereditary hypogammaglobulinemia – SOAP Notes & Clinical Use

ICD-10 Code D80.0 is utilized in SOAP notes to document the patient's symptoms, assessment findings, and treatment plans. This code is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and guiding clinical decision-making.

What Does ICD-10 Code D80.0 for Hereditary hypogammaglobulinemia Mean in SOAP Notes?

In SOAP notes, ICD-10 Code D80.0 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of hereditary hypogammaglobulinemia. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.

Treatment Options for ICD-10 Code D80.0 – Hereditary hypogammaglobulinemia

Hereditary hypogammaglobulinemia often necessitates hospitalization for management of severe infections and immunoglobulin replacement therapy.

Antibiotic Therapy:

• Intravenous immunoglobulin (IVIG) therapy, typically administered every 3-4 weeks.
• Prophylactic antibiotics such as penicillin or azithromycin may be considered.

Supportive Care:

• Regular monitoring of immunoglobulin levels and infection status.
• Vaccination against pneumococcus, Haemophilus influenzae type b, and influenza.

Infection Control:

• Strict hand hygiene practices to prevent infection spread.
• Isolation precautions during outbreaks of infectious diseases.

How to Document Symptoms of Hereditary hypogammaglobulinemia (ICD-10 D80.0) in SOAP Notes

Subjective:

• Patient reports recurrent respiratory infections over the past year.
• History of hospitalization for pneumonia.
• Family history of immunodeficiency disorders.
• Patient expresses concern about frequent illnesses.

Objective:

• Vital signs: stable, afebrile.
• Physical exam reveals signs of past infections, such as scarring.
• Laboratory results show low serum immunoglobulin levels.
• Immunological testing indicates impaired antibody response.

Secure, compliant, and built for trust

HIPAA-compliant and designed with privacy in mind, your patient’s data is protected. Focus on care while we safeguard your information.

Learn more

SOAP Note Guidelines for Diagnosing Hereditary hypogammaglobulinemia (ICD-10 Code D80.0)

Assessment:

• Diagnosis: Hereditary hypogammaglobulinemia, moderate severity.
• ICD-10 Code: D80.0.
• Contributing factors: Genetic predisposition and recurrent infections.

Plan:

• Initiate IVIG therapy every 3-4 weeks.
• Consider prophylactic antibiotics for recurrent infections.
• Educate patient on infection prevention strategies.
• Schedule follow-up in 4 weeks to reassess immunoglobulin levels.

Treatment & Plan Section for ICD-10 Code D80.0 – Hereditary hypogammaglobulinemia

• Administer IVIG therapy as per protocol.
• Implement prophylactic antibiotic regimen.
• Educate patient on recognizing signs of infection.
• Monitor immunoglobulin levels and adjust treatment as necessary.

Using ICD-10 Code D80.0 for Hereditary hypogammaglobulinemia in Billing & SOAP Note Compliance

• Ensure accurate documentation of symptoms and clinical findings.
• Use D80.0 in appropriate clinical settings, including outpatient and inpatient care.
• Align treatment plans with clinical guidelines to support billing.
• Document all relevant patient education and follow-up plans.

Related ICD-10 Codes Often Used with Hereditary hypogammaglobulinemia

• D80.1 – Selective immunoglobulin A deficiency
• D80.2 – Common variable immunodeficiency
• D80.3 – Immunodeficiency with increased IgM
• D80.4 – Immunodeficiency with increased IgG

ICD-10 Code D80.0 in Medical Billing and Insurance for Hereditary hypogammaglobulinemia

ICD-10 Code D80.0 is critical for billing in hospital, ER, or infectious disease care settings, ensuring appropriate reimbursement for services rendered.

Billing Notes:

• Document all relevant clinical findings to support the use of D80.0.
• Use this code in conjunction with other relevant codes for comprehensive billing.
• Ensure that treatment plans are clearly outlined in the medical record.

Common CPT Pairings: